反応式
C(OC1C=CN([C:15]2[CH:20]=[CH:19][C:18]([O:21]CCN(C)C)=[CH:17][CH:16]=2)C(=O)C=1)C1C=CC=CC=1.C(OC1C=CNC(=O)C=1)C1C=CC=CC=1.[F:43][C:44]1[CH:58]=[CH:57][C:47]([CH2:48][O:49][C:50]2[CH:55]=[CH:54][NH:53][C:52](=[O:56])[N:51]=2)=[CH:46][CH:45]=1>>[F:43][C:44]1[CH:58]=[CH:57][C:47]([CH2:48][O:49][C:50]2[CH:55]=[CH:54][N:53]([C:15]3[CH:20]=[CH:19][C:18]([OH:21])=[CH:17][CH:16]=3)[C:52](=[O:56])[N:51]=2)=[CH:46][CH:45]=1参加物
4
実験手順
Steps (3) and (4) of Example 1 were repeated except that 4-benzyloxy-1H-pyridin-2-one which was used in Step (3) of Example 1 was replaced with 4-(4-fluorobenzyloxy)-1H-pyrimidin-2-one, to provide the title compound.
出典と根拠
- ORDレコード
- ord-e56c0d021ff44232a5d711bf5c79d02b
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07732456B2
関連ノート
読み込み中…